KR960005459B1 - Moisturizing cosmetics - Google Patents
Moisturizing cosmetics Download PDFInfo
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- KR960005459B1 KR960005459B1 KR1019870014836A KR870014836A KR960005459B1 KR 960005459 B1 KR960005459 B1 KR 960005459B1 KR 1019870014836 A KR1019870014836 A KR 1019870014836A KR 870014836 A KR870014836 A KR 870014836A KR 960005459 B1 KR960005459 B1 KR 960005459B1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4993—Derivatives containing from 2 to 10 oxyalkylene groups
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/03—Liquid compositions with two or more distinct layers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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Abstract
내용 없음.No content.
Description
본 발명은 화장품, 더 상세하게는 지속성이 있는 높은 보습(保濕)효과를 보유하는 화장품에 관한 것이다.The present invention relates to cosmetics, and more particularly cosmetics having a high moisturizing effect with sustainability.
정상적인 피부의 각질층에는 보통 10~20%의 수분이 함유되어 있어 탄력성 및 유연성을 주며 보호기능을 유지하나 이것이 온도, 습도 등의 외부환경의 변화로 수분함량이 10%이하로 되면, 건조피부라고 불리는 상태로 되어 피부는 탄력성이나, 보호기능을 상실하여 여러 가지의 피부문제의 원인으로 되는 것이 알려지고 있다.The stratum corneum of normal skin usually contains 10-20% of moisture, which gives elasticity and flexibility and maintains protection.However, when moisture content is less than 10% due to changes in external environment such as temperature and humidity, it is called dry skin. It is known that the skin becomes elastic and loses its protective function, causing various skin problems.
이와 같은 건조피부를 막고 혹은 정상적인 피부상태로 회복시킬 목적으로서, 친수성의 보습제를 화장품에 배합하는 것이 행하여지고 있다. 통상적으로는 사용되어온 친수성 보습제로서는, 폴리에틸렌 클리콜, 폴리프로필렌글리콜, 디프로필렌글리콜, 프로필렌글리콜, 부틸렌글리콜 등의 폴리올계 화합물, 글리세린, 솔비톨, 말티톨, 아미노산, 피롤리돈 카르복실산나트륨, 요소, 유산, 히아루론산, 콜라겐 등이다. 그러나, 이들의 보습제는 친수성이 높기 때문에, 정상적인 피부에 있어서는 각질층 내부로 침투되지 않고 피부상에 잔류하여 부적합하고, 일시적인 보습효과만으로 나타낸다.In order to prevent such dry skin or to restore normal skin condition, a hydrophilic moisturizer is blended into cosmetics. Commonly used hydrophilic humectants include polyol compounds such as polyethylene glycol, polypropylene glycol, dipropylene glycol, propylene glycol, butylene glycol, glycerin, sorbitol, maltitol, amino acids, sodium pyrrolidone carboxylate, urea , Lactic acid, hyaluronic acid, collagen. However, since these moisturizing agents have high hydrophilicity, normal skin does not penetrate into the stratum corneum, remains on the skin, is inadequate, and exhibits only a temporary moisturizing effect.
이러한 실정이 있어서, 본 발명자 등은 지속성이 있고, 높은 보습효과를 보유하는 화장품을 얻기 위하여 예의 연구한 결과, 실온에서 액체상의 디글리세라이드와 폴리올계 보습제를 함께 사용하여 배합하면, 각각 단독으로서 사용하였을 때보다 높은 보습효과를 나타낸다. 또한, 이 효과의 지속성이 상승적(相乘的)으로 증대하는 것을 발견하여 본 발명을 완성하였다.In this situation, the present inventors have studied diligently to obtain a cosmetic having a long-lasting and high moisturizing effect. As a result, when the compound is used together with a liquid diglyceride and a polyol moisturizer at room temperature, each of them is used alone. It shows a higher moisturizing effect than when done. In addition, the present inventors have found that the persistence of this effect increases synergistically, thereby completing the present invention.
본 발명은 (A)실온에서 액체상인 디글리세라이드 및 (B)실온에서 (A)성분에 자유로이 용해되는 폴리올계 보습성분을 함유하는 화장품을 제공하는 것이다.The present invention provides a cosmetic comprising (A) a diglyceride which is liquid at room temperature and (B) a polyol moisturizing component which is freely dissolved in (A) component at room temperature.
본 발명에서 사용되는 (A)성분은 실온에서 액체상인 디글리세라이드로서는 융점이 20℃이하의 것이 사용된다. 이와 같은 성분은 글리세린 지방산의 에스테르화에 의해 얻어진 디에스테르를 60%이상 함유하는 지방산의 글리세린 에스테르의 분리 또는 정제하거나, 천연의 동물 또는 식물의 유질 글리세롤리스하거나, 고급지방산-고급알코올에스테르를 분자증류, 용매추출 등에 의해 글리세롤리스하여 얻어진다. 이들 중에서 디(2-에틸헥산산)글리세린 에스테르, 디옥탄산글리세린에스테르, 디올레인산글리세린에스테르가 특히 바람직하다. (A)성분의 디글리세라이드는 화장품중에 1~50중량%, 바람직하기로는 5~25중량%배합된다.As (A) component used by this invention, the thing of melting | fusing point 20 degrees C or less is used as diglyceride which is liquid form at room temperature. Such components may be isolated or purified from glycerin esters of fatty acids containing 60% or more of the diester obtained by esterification of glycerin fatty acids, oily glycerol of natural animals or plants, or molecular distillation of higher fatty acid-higher alcohol esters. And glycerol by solvent extraction or the like. Of these, di (2-ethylhexanoic acid) glycerin ester, dioctanoic acid glycerin ester and dioleic acid glycerin ester are particularly preferable. The diglyceride of (A) component is 1-50 weight% in cosmetics, Preferably it is 5-25 weight%.
(B) 성분의 폴리올계 보습성분은 (A)성분의 디글리세라이드와 실온에서 임의의 비율로 혼합가능한 것이 필요하다. 이들 (B)성분으로서는 폴리에틸렌글리콜, 폴리 프로필렌글리콜, 디프로필렌글리콜, 프로필렌글리콜, 부틸렌글리콜, 히드록시프로필에테르화 글리코리피드에스테르(PSL)등을 들 수가 있다. 이들 중에서도 (C)성분의 친수성 보습성분과의 용해 특성을 고려하면 디프로필렌글리콜, 부틸렌글리콜이 특히 바람직하다. 또 다음의 일반식으로서 표시되는 PSL이 바람직하게 사용될 수 있다.The polyol type moisturizing component of component (B) needs to be mixed with the diglyceride of component (A) at any ratio at room temperature. Examples of these (B) components include polyethylene glycol, polypropylene glycol, dipropylene glycol, propylene glycol, butylene glycol, hydroxypropyl etherified glycolipide ester (PSL), and the like. Among these, dipropylene glycol and butylene glycol are particularly preferable in consideration of dissolution characteristics of the component (C) with the hydrophilic moisturizing component. Moreover, PSL represented as the following general formula can be used preferably.
상기 식에서, R1은 CH3또는 H를 나타내고, R1이 CH3일 때, R2는 탄소수 11 내지 15의 포화 또는 불포화의 탄화수소기를 나타내며, R1이 H일 때는 R2는 탄소수 12 내지 16의 포화 또는 불포화의 탄화수소기를 나타내며,Wherein R 1 represents CH 3 or H, and when R 1 is CH 3 , R 2 represents a saturated or unsaturated hydrocarbon group having 11 to 15 carbon atoms, and when R 1 is H, R 2 represents 12 to 16 carbon atoms. A saturated or unsaturated hydrocarbon group of
A는를 나타내며, R3은 탄소수 1내지 20의 포화 또는 불포화 탄화수소기 또는 (A)hH를 나타내며, a, b, c, d, e, f, g, h는 그의 합계가 1~60의 정수를 나타낸다.A is R 3 represents a saturated or unsaturated hydrocarbon group having 1 to 20 carbon atoms or (A) h H, and a, b, c, d, e, f, g and h each represent an integer of 1 to 60. Indicates.
(B) 성분의 폴리올계 보습성분은 화장품 중에 2~90중량%, 바람작하기로는 5~50중량% 배합된다. 배합량이 2중량%미만이면, 본 발명의 효과가 발휘되지 않고, 90중량%를 초과하여 사용하면 사용된 양에 비례하는 보습지속효과의 증대는 볼 수없다. 또 (A)성분과 (B)성분의 혼합비율은 임의이나, (A)/(B)가 1/2근처가 바람직하다.The polyol moisturizing component of component (B) is 2 to 90% by weight, preferably 5 to 50% by weight in cosmetics. If the blending amount is less than 2% by weight, the effect of the present invention is not exerted, and if it is used in excess of 90% by weight, the increase in the moisturizing sustaining effect proportional to the amount used is not seen. Moreover, although the mixing ratio of (A) component and (B) component is arbitrary, (A) / (B) is near 1/2.
또 (C)성분의 친수성 보습성분으로서는 글리세린, 솔비톨, 말티톨, 아미노산, 피롤리돈카르복실산나트륨, 요소, 유산 및 히아루론산 등의 천연보습제 및 화학적 변성 콜라겐 등을 수가 있다.Examples of the hydrophilic moisturizing component of component (C) include glycerin, sorbitol, maltitol, amino acids, sodium pyrrolidone carboxylic acid, natural humectants such as urea, lactic acid and hyaluronic acid, and chemically modified collagen.
이들의 친수성 보습성분은 화장품 중에 2~25%배합된다. 본 발명의 화장품에는 본 발명의 효과를 손상하지 않는 범위에서 상기한 필수성분 이외에 화장품 성분으로서, 일반적으로 사용되고 있는 여러가지 성분들이 적당하게 배합될 수 있다.These hydrophilic moisturizing ingredients are blended 2-25% in cosmetics. The cosmetics of the present invention may be suitably blended with various components generally used as cosmetic ingredients in addition to the above essential ingredients in a range that does not impair the effects of the present invention.
이들 성분으로서는 계면활성제, 전술한 이외의 보습제, 자외선 흡수제, 킬레이트화제, pH조정제, 방부제, 증점제, 색소, 향료 등을 들 수 있다.As these components, surfactant, a moisturizer other than the above-mentioned, a ultraviolet absorber, a chelating agent, a pH adjuster, a preservative, a thickener, a pigment, a fragrance | flavor, etc. are mentioned.
본 발명에 따른 화장품은 유성화장품, 유화화장품, 수성화장품 등의 임의의 제형으로 할 수가 있어서, 거친 피부, 모발의 손실 등의 보습효과를 필요로 하는 피부 화장품, 모발화장품으로서 특히 바람직하다.Cosmetics according to the present invention can be formed in any formulation such as oily cosmetics, emulsified cosmetics, aqueous cosmetics, and the like, and are particularly preferable as skin cosmetics and hair cosmetics that require moisturizing effects such as coarse skin and hair loss.
본 발명의 화장품은 높은 보습성과 보습효과의 지속성을 보유하며, 또한 경시후(經時後) 및 세정후에도 우수한 보습성을 보전하기 때문에 피부, 모발의 손질 특히 손상한 피부, 모발의 손질에 높은 효과를 표시하는 것이다.Cosmetics of the present invention have a high moisturizing effect and a long lasting effect of moisturizing effect, and also maintains excellent moisturizing properties over time and after washing, thus having a high effect on skin, hair care, especially damaged skin and hair care. To display.
다음의 실시예에 의하여 본 발명은 또 다시 상세하게 설명하는바, 본 발명은 이것에 의하여 한정되는 것은 아니다.The present invention will be further described in detail by the following examples, but the present invention is not limited thereto.
[실시예 1]Example 1
하기 표1에 표시하는 조성의 혼합물을 조제하여 그 보습지속효과를 측정하였다.The mixture of the composition shown in following Table 1 was prepared, and the moisture retention effect was measured.
[표 1]TABLE 1
*2-에틸헥산산 디글리세라이드 * 2-ethylhexanoic acid diglyceride
[시험방법][Test Methods]
상기한 시료를 일정량 앞쪽 팔뚝 안쪽부분에 도포하여 1시간 정치한 후 더운물로 세정하여, 온도 20℃, 습도 50%의 항은 항습실에 넣고, 15분 후에 각질층중의 수분 함유량을 인피던스 미터(IBS회사제품)로서 측정하였다. 2시간 후에 다시 더운물로 세정하고 그 15분 후에 동일하게 수분 함유량을 측정하였다. 그 결과를 표2에 나타냈으며 표중에는 수분함량(단위 : μυ)을 평균값(N=10)으로서 표시하였다.The sample was applied to the inside of the front forearm in a predetermined amount and left to rest for 1 hour, and then washed with hot water. The temperature of 20 ° C. and 50% humidity were placed in a humidity chamber, and after 15 minutes, the moisture content in the stratum corneum was measured by an impedance meter (IBS company Product). After 2 hours, the mixture was washed with hot water again, and after 15 minutes, the water content was measured in the same manner. The results are shown in Table 2. In the table, the moisture content (unit: μυ) is expressed as an average value (N = 10).
[결과][result]
[표 2]TABLE 2
표 2에서 명백한 바와 같이, 본 발명품 1인 디프로필렌글리콜/디글리세라이드 혼합계는 디글리세라이드, 디프로필렌글리콜 각각 단독으로 배합한 화장품에 비하여 보습효과 및 그 지속 효과가 우수하며 양자가 상승적으로 작용하고 있는 것이 입증되었다. 또한 본 발명품 2에서 (C)성분의 첨가도 유효한 것이 판명되었다.As is apparent from Table 2, the dipropylene glycol / diglyceride mixed system of the present invention 1 has a superior moisturizing effect and a sustaining effect, and synergistically acts as compared to a cosmetic formulated with diglyceride and dipropylene glycol alone. Proved to be. Moreover, in this invention 2, addition of (C) component also turned out to be effective.
[실시예 2]Example 2
하기 표3에 표시하는 조성의 크림을 제조하여 그 보습지속효과를 측정하였다.To prepare a cream of the composition shown in Table 3 below to measure the moisturizing lasting effect.
[조성][Furtherance]
[표 3]TABLE 3
*POE(20) : 20몰 옥시에틸렌기가 첨가된 폴리옥시에틸렌 * POE (20): Polyoxyethylene with 20 mol oxyethylene group added
**2-에틸헥산산디글리세라이드 10부와 옥탄산디글리세라이드 9부의 혼합물 ** Mixture of 10 parts 2-ethylhexanoic acid diglyceride and 9 parts octanoic acid diglyceride
[제조법][Manufacturing method]
상기 오일성부 1)-7)을 혼합하고, 가열용해하여 70℃로 보전하고, 한편, 상기 수상부 8)-11)을 서서히 가하여 혼합기로서 유화한다. 유화물을 열교환기에서 30℃까지 냉각하여 크림을 얻었다(본 발명품 3).The oily parts 1) -7) are mixed, dissolved in heat and maintained at 70 ° C, while the water phase parts 8) -11) are gradually added to emulsify as a mixer. The emulsion was cooled to 30 ° C. in a heat exchanger to obtain a cream (Invention 3).
비교품 6, 7도 동일하게 하여 제조하였다.Comparative Products 6 and 7 were prepared in the same manner.
[시험방법][Test Methods]
상기의 시료를 일정량 앞쪽팔뚝 안쪽부분에 도포하고 2시간 정치한 후 더운물로 세정하여 온도 20℃, 습도 40%의 항온항습실에 넣고, 15분후에 각질층중의 수분 함유량을 인피던스미터(IBS 회사제품)으로서 측정하였다. 또한 초기 더운물로 세정한 후, 1시간, 2시간 및 5시간 경과시에도 동일하게 더운 물로 세척한 후, 각질내 수분량을 측정하였다. 이 결과를 표 3에 나타냈으며, 표중에 수분함량(단위 : μυ)은 평균값(N=4)으로서 표시하였다.The sample was applied to the inside of the front forearm in a predetermined amount, left for 2 hours, washed with hot water and placed in a constant temperature and humidity chamber with a temperature of 20 ° C. and a humidity of 40%. It was measured as. In addition, after washing with the initial hot water, even after 1 hour, 2 hours and 5 hours after washing with the same hot water, the amount of water in the keratin was measured. The results are shown in Table 3, and the water content (unit: μυ) in the table is expressed as an average value (N = 4).
[결과][result]
[표 4]TABLE 4
*단위 : μυ * Unit: μυ
표 4에서 명백한 바와 같이, 본 발명품의 크림은 폴리올계 보습제 디플로필렌 글리콜, 디글리세라이드를 각각 단독으로 배합한 비교품 6,7의 크림과 비교하여 높은 보습효과가 있으며, 또한 그 지속성이 우수하여 이들의 성분이 유화계(乳化系)에 있어서도 상승적으로 작용하고 있는 것이 입증되었다.As is apparent from Table 4, the cream of the present invention has a high moisturizing effect compared to the creams of the comparative products 6 and 7 containing the polyol-based moisturizing agent diflohylene glycol and diglyceride, respectively. It has been proved that these components act synergistically even in the emulsion system.
[실시예 3]Example 3
[제조법][Manufacturing method]
상기한 처방중의 유상(油相)성분을 혼합하여 가열용해하고, 70℃로 보전한다. 상기한 수상(水相)성분도 동일하게 70℃로 가열혼합하고, 이 수상 혼합물에 앞에서 기재한 유상 혼합물을 첨가하여 혼합기로서 유화한다. 얻어진 유화물을 열교환기로서 30℃까지 냉각하여 유액을 제조하였다.The oily ingredients in the above-mentioned prescriptions are mixed, dissolved in heat, and preserved at 70 ° C. The above-mentioned water phase component is heat-mixed similarly to 70 degreeC, and the oil phase mixture mentioned above is added to this water phase mixture, and emulsified as a mixer. The emulsion obtained was cooled to 30 ° C. as a heat exchanger to prepare an emulsion.
[실시예 4]Example 4
[제조법][Manufacturing method]
올레인산디글리세라이드에 POE(20)솔비탄테트라올레이산 에스테르 및 에틸파라벤을 첨가하여 용해하고, 에탄올을 첨가하여 유상을 만든다. 또 정제수에 1,3-부틸틸렌글리콜, 디프로필렌글리콜 및 향료를 용해한 것을 수상(水相)으로 만든다. 수상 혼합물에 유상혼합물을 실온에서 첨가하고, 잘 교반하면서 나일론포로 여과하여 최종제품을 얻었다.POE (20) sorbitan tetraoleic acid ester and ethyl paraben are dissolved in oleic acid diglyceride, and ethanol is added to form an oil phase. Moreover, what dissolved 1, 3- butyl styrene glycol, dipropylene glycol, and a fragrance | flavor in purified water is made into a water phase. The oily mixture was added to the aqueous mixture at room temperature, and filtered with nylon cloth while stirring well to obtain a final product.
실시예 3,4에서 얻어진 본 발명 화장품은 어느 것이나 우수한 보습지속효과를 나타내었다.The cosmetics of the present invention obtained in Examples 3 and 4 showed excellent moisturizing sustaining effect.
본 발명의 수많은 변경 및 개량이 전술한 기재에 의해 가능하다. 따라서, 본 발명 특허청구의 범위는 여기에 특정하여 기재한 것 이외로 실시될 수 있음은 이해될 수 있다.Many modifications and improvements of the present invention are possible with the foregoing description. Accordingly, it is to be understood that the scope of the claims may be practiced otherwise than as specifically described herein.
Claims (3)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62018042A JPH0745394B2 (en) | 1987-01-28 | 1987-01-28 | Moisturizing skin cosmetics |
JP18042/1987 | 1987-01-28 |
Publications (2)
Publication Number | Publication Date |
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KR880008796A KR880008796A (en) | 1988-09-13 |
KR960005459B1 true KR960005459B1 (en) | 1996-04-25 |
Family
ID=11960626
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019870014836A KR960005459B1 (en) | 1987-01-28 | 1987-12-23 | Moisturizing cosmetics |
Country Status (11)
Country | Link |
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US (1) | US4839162A (en) |
EP (1) | EP0277335B1 (en) |
JP (1) | JPH0745394B2 (en) |
KR (1) | KR960005459B1 (en) |
CN (1) | CN1014955B (en) |
DE (1) | DE3789807T2 (en) |
ES (1) | ES2056058T3 (en) |
HK (1) | HK48095A (en) |
MY (1) | MY101703A (en) |
PH (1) | PH23914A (en) |
SG (1) | SG30547G (en) |
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KR100557196B1 (en) * | 2004-09-21 | 2006-03-03 | 엔프라니 주식회사 | Composition with high moisturing effects, method for nano-capsulating the same and cosmetic composition containing the nano-capsulated composition |
KR20090078095A (en) * | 2008-01-14 | 2009-07-17 | (주)아모레퍼시픽 | Hair setting agent composition with improved durability |
KR101221178B1 (en) * | 2006-03-31 | 2013-01-10 | (주)아모레퍼시픽 | Clear cosmetic compositions for high moisturization without emollient |
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- 1987-12-18 SG SG1995903647A patent/SG30547G/en unknown
- 1987-12-18 DE DE3789807T patent/DE3789807T2/en not_active Expired - Fee Related
- 1987-12-18 EP EP87118852A patent/EP0277335B1/en not_active Expired - Lifetime
- 1987-12-18 ES ES87118852T patent/ES2056058T3/en not_active Expired - Lifetime
- 1987-12-18 US US07/135,038 patent/US4839162A/en not_active Expired - Lifetime
- 1987-12-23 KR KR1019870014836A patent/KR960005459B1/en not_active IP Right Cessation
- 1987-12-26 MY MYPI87003253A patent/MY101703A/en unknown
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- 1988-01-26 CN CN88100344A patent/CN1014955B/en not_active Expired
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KR100557196B1 (en) * | 2004-09-21 | 2006-03-03 | 엔프라니 주식회사 | Composition with high moisturing effects, method for nano-capsulating the same and cosmetic composition containing the nano-capsulated composition |
KR101221178B1 (en) * | 2006-03-31 | 2013-01-10 | (주)아모레퍼시픽 | Clear cosmetic compositions for high moisturization without emollient |
KR20090078095A (en) * | 2008-01-14 | 2009-07-17 | (주)아모레퍼시픽 | Hair setting agent composition with improved durability |
Also Published As
Publication number | Publication date |
---|---|
DE3789807T2 (en) | 1994-12-22 |
PH23914A (en) | 1990-01-23 |
JPS63185912A (en) | 1988-08-01 |
DE3789807D1 (en) | 1994-06-16 |
SG30547G (en) | 1995-09-01 |
MY101703A (en) | 1991-12-31 |
EP0277335A3 (en) | 1988-08-24 |
CN88100344A (en) | 1988-08-10 |
EP0277335B1 (en) | 1994-05-11 |
ES2056058T3 (en) | 1994-10-01 |
EP0277335A2 (en) | 1988-08-10 |
HK48095A (en) | 1995-04-07 |
CN1014955B (en) | 1991-12-04 |
JPH0745394B2 (en) | 1995-05-17 |
US4839162A (en) | 1989-06-13 |
KR880008796A (en) | 1988-09-13 |
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